Kujawska Małgorzata, Jourdes Michael, Witucki Łukasz, Karaźniewicz-Łada Marta, Szulc Michał, Górska Agata, Mikołajczak Przemysław Ł, Teissedre Pierre-Louis, Jodynis-Liebert Jadwiga
Department of Toxicology, Poznan University of Medical Sciences, Dojazd 30, 60-631 Poznań, Poland.
Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, Œnologie, 210 Chemin de Leysotte, F-33140 Villenave d'Ornon, France.
Brain Sci. 2021 Aug 25;11(9):1127. doi: 10.3390/brainsci11091127.
Pomegranate juice (PJ) is a rich source of ellagitannins (ETs), precursors of colonic metabolite urolithin A, which are believed to contribute to pomegranate's neuroprotective effect. While many experimental studies involving PJ's role in Alzheimer's disease and hypoxic-ischemic brain injury have been conducted, our knowledge of pomegranate's effects against Parkinson's disease (PD) is very limited. Previously, we have reported that PJ treatment improved postural stability, which correlated well with enhancement of neuronal survival, protection against oxidative damage, and α-synuclein aggregation. Since olfactory and motor deficits are typical symptoms of PD, in this study, we aimed to investigate the capability of PJ to protect against olfactory, motoric, and neurochemical alterations. To evaluate its efficiency, Wistar rats were given a combined treatment with ROT (1.3 mg/kg b.w./day, s.c.) and PJ (500 mg/kg/day, p.o.) for 35 days. After this, we assessed the olfactory discrimination index (DI) and vertical and horizontal activities as well as levels of dopamine and its main metabolite 3,4-Dihydroxyphenylacetic acid (DOPAC) in the dissected midbrain of animals. Our findings provide the first evidence that PJ treatment protects against ROT-induced DA depletion in the midbrain, which correlates well with improved olfactory function and vertical activity as well as with the presence of urolithin A in the brain.
石榴汁(PJ)是鞣花单宁(ETs)的丰富来源,鞣花单宁是结肠代谢物尿石素A的前体,据信其有助于石榴的神经保护作用。虽然已经进行了许多涉及PJ在阿尔茨海默病和缺氧缺血性脑损伤中作用的实验研究,但我们对石榴对帕金森病(PD)影响的了解非常有限。此前,我们报道PJ治疗可改善姿势稳定性,这与神经元存活的增强、抗氧化损伤保护以及α-突触核蛋白聚集密切相关。由于嗅觉和运动功能障碍是PD的典型症状,在本研究中,我们旨在研究PJ预防嗅觉、运动和神经化学改变的能力。为了评估其效果,将Wistar大鼠用ROT(1.3mg/kg体重/天,皮下注射)和PJ(500mg/kg/天,口服)联合治疗35天。此后,我们评估了动物解剖中脑的嗅觉辨别指数(DI)、垂直和水平活动以及多巴胺及其主要代谢物3,4-二羟基苯乙酸(DOPAC)的水平。我们的研究结果提供了首个证据,即PJ治疗可预防ROT诱导的中脑多巴胺耗竭,这与嗅觉功能和垂直活动的改善以及脑中尿石素A的存在密切相关。